@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP505824.RALnfMdUUr6s1gFn84Z0CGuaCTIp0t1hM8ZTQBxQ9fVEA
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP505824.RALnfMdUUr6s1gFn84Z0CGuaCTIp0t1hM8ZTQBxQ9fVEA130_head
{
this:
np:hasAssertion
dgn-np:NP505824.RALnfMdUUr6s1gFn84Z0CGuaCTIp0t1hM8ZTQBxQ9fVEA130_assertion
;
np:hasProvenance
dgn-np:NP505824.RALnfMdUUr6s1gFn84Z0CGuaCTIp0t1hM8ZTQBxQ9fVEA130_provenance
;
np:hasPublicationInfo
dgn-np:NP505824.RALnfMdUUr6s1gFn84Z0CGuaCTIp0t1hM8ZTQBxQ9fVEA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP505824.RALnfMdUUr6s1gFn84Z0CGuaCTIp0t1hM8ZTQBxQ9fVEA130_assertion
a
np:Assertion
.
dgn-np:NP505824.RALnfMdUUr6s1gFn84Z0CGuaCTIp0t1hM8ZTQBxQ9fVEA130_provenance
a
np:Provenance
.
dgn-np:NP505824.RALnfMdUUr6s1gFn84Z0CGuaCTIp0t1hM8ZTQBxQ9fVEA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP505824.RALnfMdUUr6s1gFn84Z0CGuaCTIp0t1hM8ZTQBxQ9fVEA130_assertion
{
miriam-gene:3593
a
ncit:C16612
.
lld:C0010346
a
ncit:C7057
.
dgn-gda:DGNd27fb3bd5ab7888084bd9c83e6ba196c
sio:SIO_000628
miriam-gene:3593
,
lld:C0010346
;
a
sio:SIO_001121
.
}
dgn-np:NP505824.RALnfMdUUr6s1gFn84Z0CGuaCTIp0t1hM8ZTQBxQ9fVEA130_provenance
{
dgn-np:NP505824.RALnfMdUUr6s1gFn84Z0CGuaCTIp0t1hM8ZTQBxQ9fVEA130_assertion
dcterms:description
"[The study aimed to identify additional novel genetic variants in IL12B and investigated whether variants confer susceptibility to the development of Crohn's disease (CD) or ulcerative colitis (UC) in the Korean population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:23573954
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP505824.RALnfMdUUr6s1gFn84Z0CGuaCTIp0t1hM8ZTQBxQ9fVEA130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:42:38+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetv3.0rdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}